@article {4913,
	title = {Effects from easily ionized elements on silver analyte in atmospheric pressure parallel plate capacitively coupled plasma (PP-CCP)},
	journal = {Spectrochimica Acta Part B-Atomic Spectroscopy},
	volume = {55},
	number = {4},
	year = {2000},
	note = {ISI Document Delivery No.: 313BFTimes Cited: 7Cited Reference Count: 40},
	month = {Apr},
	pages = {327-338},
	type = {Article},
	abstract = {The effect of easily ionized element (EIE) matrices on analyte emission, from a parallel plate capacitively coupled plasma (PP-CCP), has been studied. NaCl and NaNO3 were used as typical matrices and the interference on Ag emission was studied as a function of the amount of EIE and applied plasma forward power. Compared with the emission signal without the presence of matrices, the presence of either NaCl or NaNO3 as a concomitant in the sample, causes an interference effect by both enhancing, and decreasing, the emission intensity depending on the amount of added EIE. The maximum signal interference, signal enhancement, was observed at 125 W plasma forward power. The degree of enhancement from an EIE decreases with increasing forward power switching to a signal depression at a forward power of 250 W. (C) 2000 Elsevier Science B.V. All rights reserved.},
	keywords = {ABSORPTION SPECTROMETRY, ATOMIC EMISSION-SPECTROMETRY, ATOMIZATION, capacitively coupled plasma, EASILY, EASILY IONIZED ELEMENT, electron energy distribution function, INTERFERENCE, IONIZABLE ELEMENT, METAL NITRATES, MICROWAVE-INDUCED PLASMA, plasma induced dissociation, SAMPLE INTRODUCTION, SODIUM, THERMAL-DECOMPOSITION},
	isbn = {0584-8547},
	url = {<Go to ISI>://000086977900002},
	author = {Rahman, M. M. and Blades, M. W.}
}
@article {7295,
	title = {DECOMPOSITION OF ORGANOARSENIC COMPOUNDS BY USING A MICROWAVE-OVEN AND SUBSEQUENT DETERMINATION BY FLOW-INJECTION HYDRIDE GENERATION ATOMIC-ABSORPTION SPECTROMETRY},
	journal = {Applied Organometallic Chemistry},
	volume = {6},
	number = {2},
	year = {1992},
	note = {ISI Document Delivery No.: HQ168Times Cited: 61Cited Reference Count: 33INTERNATIONAL CONF ON ENVIRONMENTAL AND BIOLOGICAL ASPECTS OF MAIN-GROUP ORGANOMETALS ( ICEBAMO )SEP 15-19, 1991PADUA, ITALYUNIV PADUA, ITALIAN CHEM SOC},
	month = {Apr},
	pages = {161-171},
	type = {Proceedings Paper},
	abstract = {Environmentally important organoarsenicals such as arsenobetaine, arsenocholine and tetramethylarsonium ion do not form volatile hydrides under the commonly used analytical conditions on treatment with borohydride and it has been difficult to determine their concentrations without further derivatization. This paper describes a rapid method which completely decomposes and oxidizes these arsenicals to arsenate by using potassium persulphate and sodium hydroxide with the aid of microwave energy. The quantitative decomposition of these species permits their determination at low nanogram levels, by hydride generation atomic absorption spectrometry (HG AA). A new hydride generator which has high efficiency and minimum dead volume and therefore is suitable for flow injection analysis (FIA) is also described. A system combining flow injection analysis, on-line microwave oven digestion, and hydride generation followed by atomic absorption measurement, is developed. This system is capable of performing analysis at a sample throughput of 100-120 per hour. Calibration curves were linear from 10 to 200 ng cm-3 of arsenic and the detection limit was 5 ng cm-3 for a 100-mu-l injection or 0.5 ng of arsenic. All ten organoarsenic compounds studied gave arsenate as the decomposition product, which was confirmed by using molybdenum blue photometric measurement.},
	keywords = {ABSORPTION SPECTROMETRY, arsenic, arsenobetaine, atomic, DECOMPOSITION, DETERMINATION, DISSOLUTION, ENVIRONMENT, FLOW INJECTION ANALYSIS, HYDRIDE GENERATION, IDENTIFICATION, LIQUID-CHROMATOGRAPHY, MICROWAVE OVEN DIGESTION, MUSCLE REFERENCE MATERIAL, QUANTITATION, TRACE-ELEMENTS, WATER},
	isbn = {0268-2605},
	url = {<Go to ISI>://A1992HQ16800008},
	author = {Le, X. C. and Cullen, W. R. and Reimer, K. J.}
}
